Basu H S, Pellarin M, Feuerstein B G, Deen D F, Marton L J
Department of Neurological Surgery, School of Medicine, University of California, San Francisco 94143.
Anticancer Res. 1993 Sep-Oct;13(5A):1525-32.
Based on computer modeling, physicochemical studies of spermine-DNA interactions, and cell culture experiments, we hypothesized that polyamine analogs with hydrocarbon chain lengths differing from natural polyamines and a stronger affinity for nucleic acids than spermine should have a cellular antiproliferative effect. We tested three spermine analogs with long hydrocarbon chains, 1,16-diamino-4,12-diazahexadecane (3-8-3), 1,16-bis(ethyl)amino-4,12-diazahexadecane (BE-3-8-3), and 1,15-bis(ethyl)amino-4,11-diazapentadecane (BE-3-7-3) in human brain tumor cell lines U-251 MG, SF-126, and SF-188. Analog concentrations < or = 5 microM inhibited growth and colony-forming efficiency in each cell line by treatment day 5, with significant decreases in putrescine and spermidine, but not spermine, levels. These findings suggest that potentially cytotoxic polyamine analogs can be specified on the basis of their hydrocarbon chain length and DNA affinity.
基于计算机建模、精胺与DNA相互作用的物理化学研究以及细胞培养实验,我们推测,与天然多胺相比,具有不同碳氢链长度且对核酸具有更强亲和力的多胺类似物应具有细胞抗增殖作用。我们在人脑肿瘤细胞系U - 251 MG、SF - 126和SF - 188中测试了三种具有长碳氢链的精胺类似物,即1,16 - 二氨基 - 4,12 - 二氮杂十六烷(3 - 8 - 3)、1,16 - 双(乙基)氨基 - 4,12 - 二氮杂十六烷(BE - 3 - 8 - 3)和1,15 - 双(乙基)氨基 - 4,11 - 二氮杂十五烷(BE - 3 - 7 - 3)。到处理第5天时,类似物浓度≤5 microM可抑制每个细胞系的生长和集落形成效率,腐胺和亚精胺水平显著降低,但精胺水平未降低。这些发现表明,潜在的细胞毒性多胺类似物可根据其碳氢链长度和对DNA的亲和力来确定。